87581-57-5

Upstream product

• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 619-41-0 4-(bromoacetyl)toluene 
• 123-54-6 acetylacetone 
• 38184-47-3 3,5-dimethyl-1-pyrazolylformaminidium nitrate 

Downstream Products

• 122606-21-7 2-(3,5-dimethyl-1H-pyrazol-1-yl)-1-(4-methylphenyl)ethanol 

Relevant academic research and scientific papers

Regioselective synthesis of 1,2,4-trisubstituted imidazole from a mechanistic and synthetic prospective

The highly substituted 1,2,4-trisubtituted imidazole was regioselectively synthesized via base mediated domino reaction of amidine scaffold with phenacyl bromide followed by in situ N-alkylation of imidazole. The reaction conditions were optimized in orde

Synthesis, structural and pharmacological exploration of 2-(3, 5-dimethyl-1H-pyrazol-1-yl)-acetophenone oximes and their silver complexes

Some new compounds, 2-(3,5-dimethyl-1H-pyrazol-1-yl)-4-substituted acetophenone oximes [4a–4f; here, 4-substituent = H (a), Br (b), Me (c), Cl(d), NO2 (e), F (f)] were synthesized by the reaction of 2-(3,5-dimethyl-1H-pyrazol-1-yl)-1-arylethano

Synthesis of some novel 2-(3,5-dimethyl-1H-pyrazol-1-yl)-1-arylethanols as antimicrobial agents

In search of new biologically active agents, some novel 2-(3,5-dimethyl-1H-pyrazol-1-yl)-1-arylethanols 2a-k have been synthesized and characterized on the basis of their infra-red, nuclear magnetic resonance (NMR) (1H,13C), mass spe

Synthesis and biological evaluation of some 2-(3,5-dimethyl-1H-pyrazol-1- yl)-1-arylethanones: Antibacterial, DNA photocleavage, and anticancer activities

In continuation of our efforts to find new biologically active agents, regioselective synthesis of a series of 2-(3,5-dimethyl-1H-pyrazol-1-yl)-1- arylethanones 4a-k has been achieved under facile, extremely mild and greener reaction conditions with excel